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104558

Sigma-Aldrich

1H-1,2,4-Triazole-3-thiol

97%

Synonym(s):

3-Mercapto-1,2,4-triazole

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About This Item

Empirical Formula (Hill Notation):
C2H3N3S
CAS Number:
3179-31-5
Molecular Weight:
101.13
Beilstein:
107731
EC Number:
221-656-6
MDL number:
MFCD00005229
UNSPSC Code:
12352100
PubChem Substance ID:
24846649
NACRES:
NA.22

Assay

97%

mp

221-224 °C (lit.)

solubility

H2O: soluble 50 g/L

SMILES string

Sc1nc[nH]n1

InChI

1S/C2H3N3S/c6-2-3-1-4-5-2/h1H,(H2,3,4,5,6)

InChI key

AFBBKYQYNPNMAT-UHFFFAOYSA-N

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General description

1H-1,2,4-Triazole-3-thiol is a mercapto-substituted 1,2,4-triazole ligand and exhibits tautomerism in solution. 1H-1,2,4-Triazole-3-thiol forms novel luminescent polymers with cadmium(II) salts. 1H-1,2,4-Triazole-3-thiol undergoes regioselective S-alkylation to form a series of S-substituted derivatives.

Application

1H-1,2,4-Triazole-3-thiol was used in a study to design a surface enhanced Raman scattering based probe for fast and accurate detection of DNA markers.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Lan Sun et al.
Analytical chemistry, 79(11), 3981-3988 (2007-05-01)
To provide rapid and accurate detection of DNA markers in a straightforward, inexpensive, and multiplex format, an alternative surface-enhanced Raman scattering based probe was designed and fabricated to covalently attach both DNA probing sequence and nonfluorescent Raman tags to the
Synthesis of novel 1, 3-substituted 1H-[1, 2, 4]-triazole-3-thiol derivatives.
Eliazyan KA, et al.
Heteroatom Chem., 20(7), 405-410 (2009)
Anion-induced coordination versatility of 1H-1, 2, 4-triazole-3-thiol (HtrzSH) affording a new hybrid system of cadmium (II) polymers: synthesis, structure, and luminescent properties.
Zhang RB, et al.
Crystal Growth & Design, 8(7), 2562-2573 (2008)
A histochemical study of muscles of mice infected with Trichinella spiralis.
H N Awadalla et al.
Journal of the Egyptian Society of Parasitology, 12(1), 33-39 (1982-06-01)
Effect of some new antibilharzial drugs on oxygen consumption of mouse diaphragm and liver homogenates in experimental bilharziasis.
S M Amin et al.
Journal of the Egyptian Society of Parasitology, 12(1), 107-114 (1982-06-01)
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